唾液分泌过少和牙周炎大鼠的牙周状况和下颌骨生物力学。

Noelia B Balcarcel, César A Ossola, Gastón R Troncoso, Julieta A Rodas, Julia I Astrauskas, Clarisa Bozzini, Juan C Elverdin, Javier Fernández Solari
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引用次数: 0

摘要

口腔干燥症是唾液腺功能低下的结果,严重损害了口腔软硬组织的完整性,而牙周炎是一种感染性疾病,其特点是生物膜堆积、炎症和牙槽骨吸收。目的:本研究旨在比较实验性唾液分泌过少、牙周炎以及两者结合对大鼠牙周组织和下颌骨生物力学的有害影响:材料和方法:通过双侧下颌骨下切除术诱导大鼠出现唾液分泌过少(H 组)。牙周炎(EP 组)是通过向第一下臼齿的牙龈注射 LPS(1 毫克/毫升)诱发的。第三组同时接受两种条件(H+EP 组)。通过微型计算机断层扫描和组织形态分析评估牙槽骨损失,并通过特定技术评估牙龈炎症介质。对下颌骨的生物力学特性进行了评估:结果:与对照组相比,H 组、EP 组和 H+EP 组的牙槽骨流失量同样增加。金属蛋白酶(MMP2 和 MMP9)活性在 H 组和对照组中相似,但在 EP 组和 H+EP 组中较高(MMP2:C 9644+2214,EP 34441+3336,H 5818+1532,H+EP 42673+3184;MMP9:C 5792+961,EP 14807+861,H 9295+520,H+EP 4838+1531)。与对照组相比,H组、EP组和H+EP组的其他炎症介质或多或少都有所增加,但在大多数情况下,EP组和H+EP组的炎症介质都高于H组:结论:唾液分泌过少和牙周炎都会造成牙周损伤,但唾液分泌过少也会产生生物力学改变,造成的有害影响比牙周炎更广泛。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Periodontal status and mandibular biomechanics in rats subjected to hyposalivation and periodontitis.

Xerostomia emerges as a consequence of salivary gland hypofunction, and seriously compromises the integrity of hard and soft oral tissues, whileperiodontitis is an infectious disease characterized by biofilm accumulation, inflammation and alveolar bone resorption.

Aim: The aim this study was to compare the deleterious effects caused by experimental hyposalivation, periodontitis, and the combination of both on periodontal tissues and mandibular biomechanics in rats.

Materials and method: Hyposalivation (group H) was induced through bilateral submandibulectomy. Periodontitis (group EP) was induced by injecting LPS (1 mg/ml) into the gingiva of the first lower molars. A third group was subjected to both conditions (group H+EP). Alveolar bone loss was evaluated by micro-computed tomography and histomorphometric analysis, and gingival inflammatory mediators were assessed by specific techniques. Biomechanical properties were evaluated in mandible.

Results: Alveolar bone loss increased similarly in groups H, EP and H+EP compared to control. Metalloproteinase (MMP2 and MMP9) activity was similar in H and control, but higher in groups EP and H+EP (MMP2: C 9644+2214, EP 34441+3336, H 5818+1532, H+EP 42673+3184; MMP9: C 5792+961, EP 14807+861, H 9295+520, H+EP 4838+1531). The rest of the inflammatory mediators evaluated increased in groups H, EP and H+EP to a greater or lesser extent with respect to the control, although in most cases, they were higher in groups EP and H+EP than in group H. The biomechanical properties of the mandible increased in group H compared to the other three groups.

Conclusions: Both hyposalivation and periodontitis cause periodontal damage, but hyposalivation also produces biomechanical alterations, causing more extensive deleterious effects than periodontitis.

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